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Book of Abstracts (PDF) - International Mycological Association

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IMC7 Main Congress Theme IV: POPULATION DYNAMICS AND ECOLOGY Posters<br />

1039 - Molecular ecology <strong>of</strong> Bistorta vivipara<br />

ectomycorrhiza in alpine tundra communities<br />

J.H. Sønstebø * , K. Høiland & T. Schumacher<br />

University <strong>of</strong> Oslo, Department <strong>of</strong> Biology, Division <strong>of</strong><br />

Botany and Plant Physiology, P.O. Box 1045 Blindern,<br />

0316 Oslo, Norway. - E-mail: jornso@bio.uio.no<br />

We have studied the diversity and phylogenetic affinities <strong>of</strong><br />

mycobionts <strong>of</strong> Bistorta vivipara ectomycorrhizas in four<br />

alpine tundra plant communities in Norway, using ITS1-5.8<br />

sequences as a diversity marker. ITS1-5.8 sequences<br />

obtained by direct sequencing <strong>of</strong> 114 ectomycorrhizal root<br />

tips compared with sequences from known fungal taxa<br />

showed a high diversity <strong>of</strong> fungal mycobionts, including<br />

mycobionts from a number <strong>of</strong> distantly related taxonomic<br />

groups. The composition and taxonomic specificity <strong>of</strong> the<br />

ectomycorrhizal fungi varied considerably among the study<br />

sites. This suggests that B. vivipara is capable to interact<br />

with a number <strong>of</strong> ectomycorrhizal fungal partners in its<br />

many divergent habitats <strong>of</strong> the lowlands as well as in the<br />

alpine zone. Frequent members <strong>of</strong> the B. vivipara<br />

ectomycorrhizal symbiosis include Tomentella, Russula,<br />

Inocybe, Cortinarius, Laccaria, Hebeloma, Cenococcum<br />

and some unidentified members <strong>of</strong> Sebacinaceae. The<br />

observed high abundance and diversity <strong>of</strong> Tomentella<br />

mycobionts add to the earlier observations <strong>of</strong> importance <strong>of</strong><br />

this genus as ectomycorrhizal former also in boreal forest<br />

ecosystems. The sebacinaceous ectomycorrhizal fungal<br />

partners showed affinity (95% similarity) to orchid<br />

mycorrhizal isolates from root tips <strong>of</strong> Neottia nidus-avis<br />

retrieved from GenBank.<br />

1040 - Analysing the genetic structure <strong>of</strong> Botrytis spp. in<br />

lily and tulip fields using molecular markers<br />

M. Staats * , P. van Baarlen & J.A.L. van Kan<br />

Wageningen University, Laboratory <strong>of</strong> Phytopathology, PO<br />

Box 8025, 6700 EE Wageningen, The Netherlands. - Email:<br />

Martijn.Staats@fyto.dpw.wau.nl<br />

Botrytis spp. that are pathogenic on flower bulb crops are<br />

generally assumed to be host-specific. On lily, B. elliptica<br />

produces primary necrotic lesions which potentially expand<br />

into healthy tissue. On the non-host tulip, however, B.<br />

elliptica can only cause primary necrotic lesions. The<br />

reciprocal holds true for B. tulipae, which uses tulip as its<br />

host. The mechanistic and genetic basis <strong>of</strong> host specificity<br />

<strong>of</strong> the two Botrytis species mentioned is unclear.<br />

Distinction between the species thus far relies on<br />

morphological characteristics. At this moment it is<br />

unknown to what extent sexual reproduction contributes to<br />

genetic variation in local populations <strong>of</strong> Botrytis spp. in lily<br />

and tulip fields. A sexual stage has so far been detected in<br />

B. elliptica but not in B. tulipae. The purpose <strong>of</strong> this study<br />

is to develop DNA markers to characterise the level <strong>of</strong><br />

inter- and intraspecific heterogeneity and the amount <strong>of</strong><br />

genetic recombination in B. elliptica and B. tulipae field<br />

314<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

isolates. To reach these objectives we will use a<br />

combination <strong>of</strong> sequence analysis and novel DNA<br />

fingerprinting methods. - This research is funded by the<br />

Dutch Technology Foundation STW.<br />

1041 - Molecular markers associated with virulent and<br />

avirulent phenotypes in populations <strong>of</strong> Uromyces<br />

appendiculatus from bean fields in the Central USA<br />

J.R. Steadman * , A.T. Alleyne, J.G. Fenton & K.M.<br />

Eskridge<br />

University <strong>of</strong> Nebraska, 406 Plant Sciences, Lincoln, NE<br />

68583-0722, U.S.A. - E-mail: jsteadman1@unl.edu<br />

Uromyces appendiculatus, cause <strong>of</strong> bean rust, is<br />

characterized by highly diverse virulence phenotypes. The<br />

use <strong>of</strong> race-specific rust resistance genes has been<br />

complicated by the 'boom and bust' cycle. Pinto Olathe was<br />

released as a rust resistant bean cultivar containing the Ur-<br />

6 gene in 1979. The resistance only lasted 5 years.<br />

Resistance gene pyramiding is a strategy to strengthen<br />

race-specific resistance. Phenotyping the rust population is<br />

time-consuming and costly. Pathogen variation can also be<br />

monitored by genotyping. Previous work on molecular<br />

variation in rust pathotypes have examined geographic<br />

significance <strong>of</strong> rust races and the association between<br />

resistance and virulence patterns. In the present study we<br />

monitored the changing pattern <strong>of</strong> virulence on pinto<br />

'Olathe' over the past 20 years using both molecular and<br />

phenotypic markers. A population <strong>of</strong> over 130 isolates<br />

from the Central USA representing both avirulent and<br />

virulent pathotypes on pinto Olathe were analyzed using<br />

molecular markers such as rep-PCR and RAPD-PCR.<br />

These markers were found to discriminate between rust<br />

pathogen genotypes with virulent or avirulent interactions<br />

with the Ur-6 gene. In addition, cluster analysis <strong>of</strong> the<br />

molecular data using UPGMA methods showed agreement<br />

between statistical analysis and cluster associations <strong>of</strong> these<br />

pathotypes with selected markers.<br />

1042 - Annual production <strong>of</strong> leaf-decomposing fungi in<br />

streams<br />

K. Suberkropp 1* , B.R. Methvin 1 , M.D. Carter 2 & H.S.<br />

Weyers 3<br />

1 University <strong>of</strong> Alabama, Tuscaloosa, AL, U.S.A. - 2 Noth<br />

Carolina State University, Raleigh, NC, U.S.A. - 3 U. S.<br />

Geological Survey, Dover, DE, U.S.A. - E-mail:<br />

ksuberkp@bama.ua.edu<br />

We have determined the annual production <strong>of</strong> fungi<br />

associated with decomposing leaves in seven streams in the<br />

southeastern United States using rates <strong>of</strong> acetate<br />

incorporation into ergosterol to calculate in situ growth<br />

rates and ergosterol concentrations to estimate fungal<br />

biomass. Annual fungal production ranged from 8-551<br />

g/m 2 in these streams. Fungal production was significantly

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